Fenton 1977.
Methods | Quasi‐randomised trial, 2 arms with individual randomisation. | |
Participants | 154 pregnant women with less than 14 weeks of gestation, and who had not received or were receiving treatment for a blood disorder at clinic in Cardiff, United Kingdom. | |
Interventions | Participants were divided into 2 groups according to the day in which they attended the clinic in Cardiff: group 1 received 60 mg of elemental iron (as ferrous sulphate) daily and group 2 received no iron supplement. Setting and health worker cadre: the intervention was performed by physicians at the Antenatal Clinic of the Welsh National School of Medicine at the University Hospital of Wales, Cardiff, United Kingdom. |
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Outcomes | Hb concentration, MCV, serum ferritin, serum iron and total iron binding capacity were measured at 10‐14 weeks and at term. | |
Notes | The data in the paper are presented with no SD values. No data can be extracted from the publication for this review. Gestational age at start of supplementation: early gestational age. Anaemic status at start of supplementation: mixed/unspecified anaemia status. Daily iron dose: higher daily dose (60 mg or elemental iron). Iron release formulation: normal release preparation/not specified. Iron compound: ferrous sulphate. Malaria setting: non‐malarial setting. As of 2011: Malaria: no risk. |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | High risk | By day of clinic attendance. |
Allocation concealment (selection bias) | High risk | By day of clinic attendance. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No blinding. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Laboratory outcomes but women were treated for anaemia and this may have affected results for this outcome. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | All women appear to be accounted for in the analyses; separate figures are provided for women in the control arm who received supplements. |
Selective reporting (reporting bias) | Unclear risk | There is insufficient information to permit judgement. |
Other bias | Unclear risk | No other bias apparent. |